Observational cohort study of rilpivirine (RPV) utilization in Europe

Introduction Data on safety and effectiveness of RPV from the real-world setting as well as comparisons with other NNRTIs such as efavirenz (EFV) remain scarce. Methods Participants of EuroSIDA were included if they had started a RPV- or an EFV-containing regimen over November 2011-December 2017. Statistical testing was conducted using non-parametric Mann–Whitney U test and Chi-square test. A logistic regression model was used to compare participants’ characteristics by treatment group. Kaplan–Meier analysis was used to estimate the cumulative risk of virological failure (VF, two consecutive values > 50 copies/mL). Results 1,355 PLWH who started a RPV-based regimen (11% ART-naïve), as well as 333 initiating an EFV-containing regimen were included. Participants who started RPV differed from those starting EFV for demographics (age, geographical region) and immune-virological profiles (CD4 count, HIV RNA). The cumulative risk of VF for the RPV-based group was 4.5% (95% CI 3.3–5.7%) by 2 years from starting treatment (71 total VF events). Five out of 15 (33%) with resistance data available in the RPV group showed resistance-associated mutations vs. 3/13 (23%) among those in the EFV group. Discontinuations due to intolerance/toxicity were reported for 73 (15%) of RPV- vs. 45 (30%) of EFV-treated participants (p = 0.0001). The main difference was for toxicity of central nervous system (CNS, 3% vs. 22%, p < 0.001). Conclusion Our estimates of VF > 50 copies/mL and resistance in participants treated with RPV were similar to those reported by other studies. RPV safety profile was favourable with less frequent discontinuation due to toxicity than EFV (especially for CNS). Supplementary Information The online version contains supplementary material available at 10.1186/s12981-022-00457-0.


Introduction
Rilpivirine (RPV) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) which was approved as Edurant ™ by the European Commission on 28 November 2011 for the treatment of human immunodeficiency virus type 1 (HIV-1) infection in antiretroviral treatment (ART)-naïve adult persons living with HIV (PLWH) with a baseline viral load (VL) ≤ 100,000 HIV-RNA copies/ ml. RPV has been made available over the years as the Open Access AIDS Research and Therapy *Correspondence: a.cozzi-lepri@ucl.ac.uk 1 Centre for Clinical Research, Epidemiology, Modelling and Evaluation (CREME), Institute for Global Health, University College London, Rowland Hill St, London NW3 2PF, UK Full list of author information is available at the end of the article active ingredient in several marketed fixed dose combination (FDC) tablets [1]. Although RPV in the FDC tablet formulation including emtricitabine (FTC) and tenofovir disoproxil fumarate (TDF) (Eviplera ™ ) was initially approved for ART-naïve adult PLWH with a baseline VL ≤ 100,000 copies/ml only, the indication was extended in October 2013 for ART-experienced adults who are virologically suppressed with no history of virological failure (VF).
Several randomized studies [2][3][4][5][6][7][8][9] have compared the efficacy of RPV-based regimens with that of EFV-based regimens in both the ART-naïve and ART-experienced populations. Overall, these studies have shown relatively low rates of VF at 1 year (never above 15%) with no evidence for a difference in rate of VF. However, long-term virological outcomes of these regimens have been rarely examined in real-world clinical practice across Europe [10][11][12].
The aim of this analysis was to describe the use of RPVcontaining regimens in routine clinical practice among adult PLWH followed in the EuroSIDA study. Specifically, key objectives were: (i) to evaluate factors associated with the probability of initiation of RPV-instead of EFVcontaining regimens and (ii) to describe the safety and effectiveness of RPV, including evaluation of virological response and treatment-emergent resistance-associated mutations (RAMs).

Study design
The EuroSIDA study cohort is a prospective, observational cohort of HIV-1 infected participants from 117 clinical centers across Europe, Israel and Argentina [13]. Details regarding study design and data collection are described elsewhere [https:// chip. dk/ Resea rch/ Studi es/ EuroS IDA]. Information about adverse events are collected in the EuroSIDA cohort according to the Data Collection on Adverse events of Anti-HIV Drugs (D:A:D) definitions starting from 1998 [14], and detailed information about the cause of death is collected using the Coding of Death (CoDe) algorithm [15].
Up to March 2017, source documents from the laboratories performing resistance testing were sent to the EuroSIDA coordination center and recorded RAMs were keyed into a central database. The keyed results were subsequently double checked for correctness by a second person. After March 2017 resistance test results were no longer reported to EuroSIDA because VF was infrequent and resistance testing was very rarely perfomed.

Data quality assurance
To ensure verification of collected data, an extensive quality assurance programme has been in place since EuroSIDA was initiated. Monitoring previously included on-site visits to all participating centers. However, as the study has evolved, new processes have been formulated including centralized monitoring, building on the riskbased monitoring used in clinical trials. In autumn 2014, EuroSIDA also transitioned from collecting data on paper forms to using the electronic case report system Research Electronic Data Capture [16]. More details together with the full ist of collect variables are provided here [13,17].

Study population
Participants were included if they were at least 16 years of age and they had started a RPV-containing or EFVcontaining regimen over the period November 2011 to end of December 2017. November 2011 is the earliest of the dates of market availability of RPV-containing products (Edurant ™ , the single agent tablet, or Eviplera ™ , a single tablet regimen containing RPV/TDF/FTC) within the 28 countries where RPV-containing regimens were approved and marketed for use in participants with baseline VL ≤ 100,000 copies/ml (see full list of these countries in Additional file 1).
In October 2013, Eviplera ™ was approved and marketed for use in ART-experienced adults who are virologically suppressed with no history of VF, and therefore people starting Eviplera ™ from ART-naive or switching to Eviplera ™ were also included. The last follow-up date recorded for a person in this analysis is December 31, 2017. Although FTC/RPV/tenofovir alafenamide (brand name Odefsey ™ ) was approved in the European Union in June 2016, there was no use of this formulation in participants of this analysis. Thus, RPV mentioned throughout this work refers to RPV-containing regimens, either the single agent Edurant ™ or the FDC (FTC/RPV/TDF), Eviplera ™ , while EFV refers to EFV-containing regimens, either the single agent (SUSTIVA/STOCRIN ™ ) or the FDC ATRIPLA ™ .
All PLWH who started EFV-based regimens regardless of the level of VL were included, as a comparator group, to provide a contemporary context of utilization and outcomes (i.e. rates of VF and resistance patterns). Unfortunately, the use of EFV has waned in the clinics over time and the a priori target for the minimum number of VF events in this group required for a formal comparison was never reached over the duration of the study.

Statistical analysis
Continuous variables were summarised using medians, minimums, maximums, and interquartile ranges as appropriate. Characteristics of participants who initiated RPV-or EFV-based regimens were described. Statistical testing was conducted to compare population medians (non-parametric Mann-Whitney U test) and chi-square test for proportions by treatment group. A logistic regression model was used to identify factors independently associated with the probability of starting RPV-vs. EFV-based regimens. Age, gender, weight, or body mass index (BMI), ethnicity, CD4 cell count, pre-treatment VL, mode of HIV transmission, co-infection with hepatitis B/C, HIV treatment status (naïve/experienced) were all identified as potential determinants of treatment initiation either with RPV or EFV. See Additional file 1: Table  AF1 for a detailed codebook of variables included. Unadjusted and adjusted odds ratios (ORs) of starting RPV vs. EFV were tabulated with 95% confidence intervals (CI).
Characteristics showing an association with the outcome of starting RPV with a p-value < 0.1 were considered for inclusion in the multivariable model; for categorical variables the global (type III) p-value was used to detect overall associations.
The main reason for discontinuing RPV and EFV, as reported by the treating physicians from a pre-specified list of options, were summarized and frequency compared by treatment group. Average levels of selected laboratory parameters (most recent value before stopping RPV/ EFV) were also calculated and compared.
Time to confirmed VF > 50 copies/mL in participants who started RPV-based regimens and had at least two VL measurements after starting therapy was estimated. The date of VF was defined at the time of the first of two consecutive values > 50 copies/mL after >6 months from starting the RPV-or EFV-based regimen. Due to the small number of VF events, especially in the EFV-treated group, VF and resistance accumulation analyses are only descriptive. Kaplan-Meier analysis was used to estimate the cumulative probability of VF > 50 copies/mL by 1 and 2 years with 95% CI in the RPV group alone.
There were missing data for some of the variables collected. For categorical factors, under the assumption of data missing at random, a separate group for missing values was allowed so that no participants were excluded from the analysis (the missing-indicator method). If a variable was analysed as continuous and there were missing values for this variable, participants with the missing value were instead excluded. All data were analysed using SAS version 9.4 (Cary, NC, USA).

Study population
Overall, as of December 31st, 2017, the number of participants within the labelled indication in EU for RPV (i.e. participants with a baseline VL of ≤ 100,000 copies/ml) newly initiating a RPV-containing regimen was 1,355, and the number of participants initiating an EFV-containing regimen was 333. A total of 144 (11%) of the RPV-based treated group were ART-naïve.
Additional information regarding participants included in the RPV treatment group alone are shown in Additional file 1: Table AF2. Of the 333 included participants who started an EFV-containing regimen, 178 (55%) were ART-naïve (Fig. 1). Table 1 shows the main characteristics of participants who started RPV or EFV at time of treatment initiation. Participants treated with RPV were older (median ages 48 vs. 39 years; p < 0.0001), had higher CD4 cell counts (median 566 vs. 306 cells/mm 3 ; p < 0.0001), lower HIV-RNA VL (median 1.59 vs. 4.05 log 10 copies/ml; p < 0.0001), and had been enrolled in EuroSIDA for a longer period (140.8 vs. 21.4 months; p < 0.0001). A higher proportion of participants who received RPV resided in Southern and West Central Europe (32.8% vs. 21.0% and 29.5% vs. 17.4%, respectively), with a similar proportion residing in the North (19.9% RPV, 20.4% EFV), while a far lower proportion of participants resided in Eastern Europe (2.1% vs. 23.1%; region global p = 0.0001). Other baseline characteristics and more detailed information are shown in Additional file 1: Table AF3. These differences detected by univariable analysis were confirmed in a multivariable logistic regression analysis. Adjusted Odds Ratio [aOR] for starting RPV-based vs. EFV-based regimens are shown in Table 2. Regarding the geographical distribution, after controlling for the other variables included in the model, participants treated with RPV were confimerd to be less likely to reside in East Europe (adjusted Odds Ratio [aOR]: 0.11 (95% confidence interval [CI]. 0.04-0.28; p < 0.001)) compared with West Central Europe.

ARV treatment status
Overall, in the RPV group, 144 (10.6%) participants were ART-naive and 172 (12.7%) were naïve to cART (i.e. they had never previously received a regimen including ≥ 3 ARVs); overall 1,211 individuals (89.4%) had previously taken at least one ARV drug. Additional file 1: Fig. AF1(a) shows the breakdown of the ARV treatment status of participants prior to initiating RPV-or EFV-containing regimens. A higher proportion of participants treated with RPV vs. EFV had been previously exposed to ARVs (i.e., exposure to at least 1 ARV from any class) (89.4% vs. 46.5%; p < 0.0001) and cART (i.e. exposure to ≥ 3 ARVs from any class) (87.3% vs. 42.6%; p < 0.0001) as compared to those who started EFV.
In the newly initiated RPV/EFV-based regimen, the most frequently used NRTI pair was TDF/FTC (61%) followed by ABC/3TC (33%) and ZDV/3TC (2%) with no evidence for a difference in distribution by treatment group. Approximately 5% of the RPV group also received an INSTI (i.e. RAL or DTG) (Additional file 1: Fig. AF1(b)).

Viral load and HIV drug resistance monitoring
Of the 1,355 participants who started an RPV-containing regimen, 1,184 (87.4%) had a VL measurement available in the 6 months prior to baseline. Of these, 938 (79.1%) had a VL ≤ 50 copies/ml, 235 (19.8%) had a VL between 51 and 100,000 copies/mL and 11 individuals (0.9%) had a VL > 100,000 copies/mL. In the subset of 1,302/1,355 (96.1%) RPV and 323/333 (97.0%) EFV participants who had at least two VL values during follow-up, the proportion of those who experienced VF (two consecutive HIV-RNA > 50 copies/mL) was 5.5% (71/1,302, 95% CI 4.3-6.8%) and 7.4% (24/323, 95% CI 7.4-10.9%) for RPV-and EFV-based ART, respectively. The Kaplan-Meier estimates of the cumulative probability of VF for the RPV-based group were 1.5% (95% CI 0.7-2.2%) by 1 year and 4.5% (95% CI 3.3-5.7%) by 2 years from starting the RPV-based regimen (Fig. 2). Of note, this rate was mainly driven by the treatment-experienced group in whom the overall risk of VF was 66/1211 (5.5%). Due to the small number of events in the EFV group, the Kaplan-Meier estimates for participants who started the EFV-based regimens were not performed.

Discussion
We have assessed clinical characteristics, virological outcomes, emergence of RAMs and adverse events during follow up, for individuals who initiated a RPVor EFV-containing regimen. Over the period November 2011-December 2017, the majority (99%) of individuals initiating a RPV-containing regimen, did so with a HIV-RNA ≤ 100,000 copies/ml, in accordance with the approved EU labelled indication. Overall, although a formal comparison with EFV was not perfomed as by the pre-specified protocol, we found that rate of VF and development of RAMs by 2 years was low in the RPV group (23%) and rates were comparable to those experienced by PLWH who started EFV (33%). Of note, the frequency of discontinuation due to toxicity was lower in RPV vs. EFV (15% versus 30%).
There were some key differences in the case-mix of participants who started RPV-based regimens vs. EFVbased regimens in the study. First, there were significant regional differences with participants treated with RPV less likely to reside in East Europe compared with West Central Europe. Participants starting RPV-based regimens also typically had lower HIV-1 RNA levels and higher CD4 counts. Interestingly, there was no evidence for a difference in the prevalence of ART-naïve participants by treatment group after controlling for other key predictors.
Protocol targets for the number of VF required to perform a formal comparison could not be achieved because the number of participants who started EFV and recruited in the study decreased over time, most likely because the European treatment guidelines starting from 2015 ceased to recommend its use. However, some conclusions might be drawn by comparing the VF estimates in the RPV group with those of historical data [2-9, 14, 15]. In the majority of the previously conducted randomized comparisons, EFV was the control group and, in these settings, no difference in rate of VF was found between RPV and EFV overall or in subsets of individuals (e.g. people with HBV co-infection). Even Table 3 Reasons for discontinuing RPV or EFV Reasons listed are those for stopping either RPV or EFV 1 Denominator is the number of participants who have discontinued RPV (n = 498) 2 Denominator is the number of participants who have discontinued EFV (n = 148) Reasons for discontinuation can be found at https:// hicdep. org/ Wiki/v/ 9/ pt/4/ Table/  when considering the upper limit of confidence interval of 6% VF by 2 years for RPV recipients, this estimated rate is lower than that observed in participants enrolled in randomized studies [2][3][4][5][6][7][8][9]. The slight discrepancy in the rate of RPV VF in our cohort vs. that observed in the ECHO/THRIVE trials (5.4% failure by 1 year) might be due to the fact that the trial participants used single compound combination therapy while in our analysis a large proportion of participants used the FDC Eviplera ™ . Indeed, Study GS-US-264-0106 (SPIRIT), conducted in participants with VL ≤ 50 copies/mL who were switched to RPV-based FDC, showed a more comparable rate of VF of 11% by 1 year [9]. Of note, most of these clinical trials were conducted in ART-naïve participants, while our analysis uses the data of participants who started RPV when they were ART-experienced, comprising a selected population at reduced risk of VF. A summary of the rates of RPV VFs by 1 year in EuroSIDA as well as in the mentioned randomized clinical trials [2][3][4][5][6][7][8][9] is shown in a Additional file 1: Table AF5 which also includes other estimates from real-world studies in Europe [10][11][12].
Resistance test results were available for a small subset (21%) of RPV participants who experienced VF. Detection of genotypic resistance in this subset was infrequent and the profile of individual treatment-emergent NRTI and NNRTI RAMs among participants on RPV-based regimens was that expected in those failing these combinations. Participants in whom resistance mutations were detected at time of failure did not have a baseline resistance test available. However, the prevalence of baseline NNRTI-associated resistance estimated from those with available data was lower than 20%; thus, we can speculate that for the majority of participants, the mutations detected at VF have been newly acquired rather than preexist, which is consistent with the results of previously published reports [2][3][4][5][6][7][8][9]. Nevertheless, in Study GS-US-264-0110 (STaR), 6% of participants starting RPV in FDC developed HIV-drug resistance by 96 weeks of follow-up, which was mainly seen within the first 48 weeks [5][6][7]; of note, this rate was significantly higher than that seen for EFV (2.3%), but our data did not confirm this finding.
Overall 37% of participants initiating RPV discontinued the drug compared to 44% in those initiating EFV. RPV led to less discontinuation due to toxicity (14.7% vs. 30.4%), especially for CNS toxicity, which is a recognized side effect for EFV [18]. There was a higher probability of stopping RPV due to physician's choice (33.5% vs. 15.5%), possibly indicating modifications due to proactive switches, risk of drug to drug interactions, problems associated with food intake, planning of pregnancy or possibly reported poor adherence. Although misclassification of the reason for stopping is always possible, treatment toxicity and VF are specifically listed as one of the reasons in EuroSIDA RedCap, so it is unlikely that those were recorded as 'physician's choice' . Moreover, only adverse events leading to drug discontinuations are recorded in EuroSIDA and a number of low grade adverse events are not routinely recorded. Of note, because EFV has a more recognized toxicity profile, it is possible that for a given symptom severity EFV had a greater risk of being discontinued than RPV. However, it could be equally argued that because RPV was a newer drug, monitoring of toxicity might have been stricter for participants receiving RPV. The frequency of discontnuations due to VF were higher in the RPV group but this   was not analysed by means of the more reliable analysis looking at the actual viral load values. Drug formulation are known to also have an effect on adherence and hence effectiveness/outcomes. Nevertheless, cases in which drugs were used as FDC vs. combinations of single compounds have been treated equally in this analysis. In addition, no difference in laboratory abnormalities between RPV and EFV when comparing the proportion of participants with a value below/above normal values for ALT and AST were found. These data confirm the safety profile of RPV observed in the trials [2][3][4][5][6][7][8][9]. This study has several limitations. First, since allocation of treatment in observational studies is not randomised, treatment decisions may be influenced by prognostic factors and the resulting imbalance in the underlying risk profile between groups can generate biased results. Some of these unmeasured confounders may include adherence to treatment, minor symptoms and socio-demographic factors. Importantly, most comparisons were conducted in unadjusted analysis or, like for the virological endpoint, using historical data so measured confounding cannot be excluded either. The slow recruitment of new participants starting EFV could not be predicted and ultimately limited the ability to perform a formal comparison between the two groups. Moreover, resistance data collection stopped in EuroSIDA in March 2017 so cumulative estimates of resistance detection are likely to be underestimated. Finally, the analysis includes EuroSIDA data collected up to 2018 and this is the reason why more contemporary RPV regimens such as those based on TAF have not been included.
Key strengths of the study are the real-world setting, its large sample size (larger than any other cohort study published to date for the ART-experienced population treated with RPV-based regimens) and the average two years of virological follow-up. Another strength is the prospective nature of the EuroSIDA cohort so that reverse causality is unlikely to have occurred for the main endpoint of VF/development of resistance as this temporarily occured after the initiation of RPV or EFV. Of note, the results and conclusions from this analysis are not directly generalizable outside of the subset of Euro-SIDA participants satisfying the inclusion criteria for this analysis.
In conclusion, RPV was used in accordance with the approved indication for RPV-containing regimen in Europe. Even in the worst-case scenario (upper limit of confidence interval) our real-world estimate of the rate of VF > 50 copies/mL in participants treated with RPV were similar to those reported by other European cohorts and even lower than the rates observed in randomized clinical studies. Based on available data, the proportion of participants who acquired NNRTI resistance-associated mutations was low in the few participants who experienced VF in both treatment groups. Importantly, this data also confirm the safety profile of RPV, with less frequent discontinuation due to toxicity than EFV (especially for CNS toxicity) and no evidence for a difference in liver toxicity, consistent with what was observed in randomized trials. The potential low cost and dose of the drug means that rilpivirine can potentially be manufactured at a low price. Moreover, its long half-life suggests the potential for monthly dosing via nonoral routes, with promising early results from studies of a long-acting injectable formulation. These characteristics still currently make rilpivirine an attractive drug for resourcelimited settings.

Learn more biomedcentral.com/submissions
Ready to submit your research Ready to submit your research ? Choose BMC and benefit from: ? Choose BMC and benefit from: